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Muscle Energy Technique Versus Mulligan Mobilization on Forward Head Posture

Muscle Energy Technique Versus Mulligan Mobilization on Forward Head Posture: a Randomized Controlled Trial

Status
Not yet recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06732557
Enrollment
60
Registered
2024-12-13
Start date
2024-12-31
Completion date
2025-02-28
Last updated
2024-12-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Forward Head Posture

Keywords

forward head posture, Mulligan Mobilization, Muscle energy technique

Brief summary

sixty patients with forward head posture will be randomized to three groups Group A: will receive traditional treatment ( isometric exercise for deep neck flexors plus sub occipital release). Group B: will receive traditional treatment plus muscle energy technique for upper trapezius, elevator scapulae and sternocleidomastoid. Group C: will receive traditional treatment plus mulligan mobilization

Interventions

Isometric exercise for deep neck flexors and sub occipital release

OTHERmuscle energy technique

Muscle energy technique for upper trapezius, elevator scapulae and sternocleidomastoid

OTHERMulligan Mobilization

Mulligan mobilization in the form of SNAGS for rotation, lateral flexion, extension and flexion

Sponsors

Cairo University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 45 Years
Healthy volunteers
No

Inclusion criteria

* Age between 18 to 45 years * Non specific neck pain reproduced by neck movement * Neck pain at least within the last three months * Limitation in cervical range of motion

Exclusion criteria

* cervical spine surgery or injury * neurologic deficits, infection or inflammation * cervicogenic headache

Design outcomes

Primary

MeasureTime frameDescription
PainBefore the first session and at the end of the treatment program ( one month)Pain will be measured by visual analogue scale which is a valid and reliable scale for measuring pain starts with zero (represents no pain) and ends with 10 (represents maximum pain).
Cervical range of motionBefore the first session and after the end of the treatment program ( one month)Cervical range of motion in will be measured by cervical range of motion basic assessment device (CROM) the angle of cervical range of motion will be recorded in degrees to determine the limitation in range of motion
Disability measurementBefore the first session and after the end of the treatment program ( one month)Disability will be measured by neck disability index(NDI) is a valid and reliable scale. The NDI consists of ten questions in the following domains: Pain Intensity, Personal Care, Lifting, Reading, Headaches, Concentration, Work, Driving, Sleeping, and Recreation. Scoring: Each question contains six answer choices, scored from 0 (no disability) to 5 (complete disability). All section scores are then totaled. Scoring is reported on a 0-50 scale, 0 being the best possible score and 50 being the worst. Alternately, the score can be reported from 0-100. The score is often reported as a percentage (0-100%).
Cervicovertebral angleBefore the first session and after the end of the treatment program ( one month)Cervicovertebral angle (CVA) Will be measure by kinovea: Normal range is between 55 and 86, If the angle is less than 50 degrees, it will be considered to be FHP. Adhesive markers (8 mm in diameter) will be placed on the participant's C7 spinous process and tragus of the ear. The physical therapist will observe the participant from the lateral side while standing and then take a picture of the participant from a fixed distance (75 cm) and height (150 cm), then with the help of an application sealed by a password which is called KINOVEA, the angle will be measured by placing each vector as following a line from the tragus of the ear to the C7 spinous process and another horizontal line through the C7 spinous. The angle will be recorded in degrees

Contacts

Primary ContactRadwa fayek Lecturer at Basic Science Department MTI University, Doctoral
radwa26fayek@yahoo.com02-01004466229

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026